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Compile Data Set for Download or QSAR

Found 149 hits with Last Name = 'suo' and Initial = 'fz'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM256459
PNG
(US10329256, Example 3 | US9487512, 3 | US9944601, ...)
Show SMILES C1[C@@H](NC2CCNCC2)[C@@H]1c1ccccc1 |r|
Show InChI InChI=1S/C14H20N2/c1-2-4-11(5-3-1)13-10-14(13)16-12-6-8-15-9-7-12/h1-5,12-16H,6-10H2/t13-,14+/m0/s1
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n/an/a 24n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50445346
PNG
(CHEMBL3104250)
Show SMILES CC(=NNC(=O)c1cccc(c1)S(=O)(=O)N1CCOCC1)c1cc(Cl)ccc1O |w:2.2|
Show InChI InChI=1S/C19H20ClN3O5S/c1-13(17-12-15(20)5-6-18(17)24)21-22-19(25)14-3-2-4-16(11-14)29(26,27)23-7-9-28-10-8-23/h2-6,11-12,24H,7-10H2,1H3,(H,22,25)
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n/an/a 24n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451592
PNG
(CHEMBL4212776)
Show SMILES Oc1ccc(Cl)cc1\C=N\NC(=O)c1cccc(c1)S(=O)(=O)N1CCOCC1
Show InChI InChI=1S/C18H18ClN3O5S/c19-15-4-5-17(23)14(10-15)12-20-21-18(24)13-2-1-3-16(11-13)28(25,26)22-6-8-27-9-7-22/h1-5,10-12,23H,6-9H2,(H,21,24)/b20-12+
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50158869
PNG
(CHEMBL3786182 | US10836743, Compound GSK-2879552 |...)
Show SMILES OC(=O)c1ccc(CN2CCC(CN[C@@H]3C[C@H]3c3ccccc3)CC2)cc1 |r|
Show InChI InChI=1S/C23H28N2O2/c26-23(27)20-8-6-18(7-9-20)16-25-12-10-17(11-13-25)15-24-22-14-21(22)19-4-2-1-3-5-19/h1-9,17,21-22,24H,10-16H2,(H,26,27)/t21-,22+/m0/s1
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Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451589
PNG
(CHEMBL4204049)
Show SMILES CCN(CC)c1ccc(\C=N\NC(=O)CN[C@@H]2C[C@H]2c2ccc(F)c(F)c2)c(O)c1 |r|
Show InChI InChI=1S/C22H26F2N4O2/c1-3-28(4-2)16-7-5-15(21(29)10-16)12-26-27-22(30)13-25-20-11-17(20)14-6-8-18(23)19(24)9-14/h5-10,12,17,20,25,29H,3-4,11,13H2,1-2H3,(H,27,30)/b26-12+/t17-,20+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451591
PNG
(CHEMBL4208387)
Show SMILES CCOc1cccc(\C=N\NC(=O)CN[C@@H]2C[C@H]2c2ccc(F)c(F)c2)c1O |r|
Show InChI InChI=1S/C20H21F2N3O3/c1-2-28-18-5-3-4-13(20(18)27)10-24-25-19(26)11-23-17-9-14(17)12-6-7-15(21)16(22)8-12/h3-8,10,14,17,23,27H,2,9,11H2,1H3,(H,25,26)/b24-10+/t14-,17+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451583
PNG
(CHEMBL4216474)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1cc(O)ccc1O |r|
Show InChI InChI=1S/C19H19F2N3O3/c1-10(13-7-12(25)3-5-18(13)26)23-24-19(27)9-22-17-8-14(17)11-2-4-15(20)16(21)6-11/h2-7,14,17,22,25-26H,8-9H2,1H3,(H,24,27)/b23-10+/t14-,17+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451590
PNG
(CHEMBL4215722)
Show SMILES COc1ccc(\C=N\NC(=O)CN[C@@H]2C[C@H]2c2ccc(F)c(F)c2)c(O)c1 |r|
Show InChI InChI=1S/C19H19F2N3O3/c1-27-13-4-2-12(18(25)7-13)9-23-24-19(26)10-22-17-8-14(17)11-3-5-15(20)16(21)6-11/h2-7,9,14,17,22,25H,8,10H2,1H3,(H,24,26)/b23-9+/t14-,17+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451576
PNG
(CHEMBL4205178)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1ccccc1 |r|
Show InChI InChI=1S/C19H19F2N3O/c1-12(13-5-3-2-4-6-13)23-24-19(25)11-22-18-10-15(18)14-7-8-16(20)17(21)9-14/h2-9,15,18,22H,10-11H2,1H3,(H,24,25)/b23-12+/t15-,18+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451582
PNG
(CHEMBL4214175)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1ccccc1O |r|
Show InChI InChI=1S/C19H19F2N3O2/c1-11(13-4-2-3-5-18(13)25)23-24-19(26)10-22-17-9-14(17)12-6-7-15(20)16(21)8-12/h2-8,14,17,22,25H,9-10H2,1H3,(H,24,26)/b23-11+/t14-,17+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451578
PNG
(CHEMBL4209901)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1ccc(Br)cc1 |r|
Show InChI InChI=1S/C19H18BrF2N3O/c1-11(12-2-5-14(20)6-3-12)24-25-19(26)10-23-18-9-15(18)13-4-7-16(21)17(22)8-13/h2-8,15,18,23H,9-10H2,1H3,(H,25,26)/b24-11+/t15-,18+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451577
PNG
(CHEMBL4203790)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C19H18ClF2N3O/c1-11(12-2-5-14(20)6-3-12)24-25-19(26)10-23-18-9-15(18)13-4-7-16(21)17(22)8-13/h2-8,15,18,23H,9-10H2,1H3,(H,25,26)/b24-11+/t15-,18+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451596
PNG
(CHEMBL4203515)
Show SMILES CCN(CC)c1ccc(\C=N\NC(=O)CN[C@@H]2C[C@H]2c2ccc(F)c(F)c2)cc1 |r|
Show InChI InChI=1S/C22H26F2N4O/c1-3-28(4-2)17-8-5-15(6-9-17)13-26-27-22(29)14-25-21-12-18(21)16-7-10-19(23)20(24)11-16/h5-11,13,18,21,25H,3-4,12,14H2,1-2H3,(H,27,29)/b26-13+/t18-,21+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451587
PNG
(CHEMBL4214864)
Show SMILES Fc1ccc(cc1F)[C@@H]1C[C@H]1NCC(=O)N\N=C\c1cccs1 |r|
Show InChI InChI=1S/C16H15F2N3OS/c17-13-4-3-10(6-14(13)18)12-7-15(12)19-9-16(22)21-20-8-11-2-1-5-23-11/h1-6,8,12,15,19H,7,9H2,(H,21,22)/b20-8+/t12-,15+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451585
PNG
(CHEMBL4217387)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1cc(F)ccc1O |r|
Show InChI InChI=1S/C19H18F3N3O2/c1-10(13-7-12(20)3-5-18(13)26)24-25-19(27)9-23-17-8-14(17)11-2-4-15(21)16(22)6-11/h2-7,14,17,23,26H,8-9H2,1H3,(H,25,27)/b24-10+/t14-,17+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451594
PNG
(CHEMBL4212293)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1cccc(N)c1O |r|
Show InChI InChI=1S/C19H20F2N4O2/c1-10(12-3-2-4-16(22)19(12)27)24-25-18(26)9-23-17-8-13(17)11-5-6-14(20)15(21)7-11/h2-7,13,17,23,27H,8-9,22H2,1H3,(H,25,26)/b24-10+/t13-,17+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451580
PNG
(CHEMBL4202897)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1ccc(cc1)[N+]([O-])=O |r|
Show InChI InChI=1S/C19H18F2N4O3/c1-11(12-2-5-14(6-3-12)25(27)28)23-24-19(26)10-22-18-9-15(18)13-4-7-16(20)17(21)8-13/h2-8,15,18,22H,9-10H2,1H3,(H,24,26)/b23-11+/t15-,18+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451586
PNG
(CHEMBL4209645)
Show SMILES Fc1ccc(cc1F)[C@@H]1C[C@H]1NCC(=O)N\N=C\c1ccco1 |r|
Show InChI InChI=1S/C16H15F2N3O2/c17-13-4-3-10(6-14(13)18)12-7-15(12)19-9-16(22)21-20-8-11-2-1-5-23-11/h1-6,8,12,15,19H,7,9H2,(H,21,22)/b20-8+/t12-,15+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451595
PNG
(CHEMBL4211184)
Show SMILES Oc1ccc(Br)cc1\C=N\NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1 |r|
Show InChI InChI=1S/C18H16BrF2N3O2/c19-12-2-4-17(25)11(5-12)8-23-24-18(26)9-22-16-7-13(16)10-1-3-14(20)15(21)6-10/h1-6,8,13,16,22,25H,7,9H2,(H,24,26)/b23-8+/t13-,16+/m0/s1
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Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451581
PNG
(CHEMBL4214311)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1cccc(N)c1 |r|
Show InChI InChI=1S/C19H20F2N4O/c1-11(12-3-2-4-14(22)7-12)24-25-19(26)10-23-18-9-15(18)13-5-6-16(20)17(21)8-13/h2-8,15,18,23H,9-10,22H2,1H3,(H,25,26)/b24-11+/t15-,18+/m0/s1
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n/an/a 423n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451588
PNG
(CHEMBL4206303)
Show SMILES Oc1ccc(Cl)cc1\C=N\NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1 |r|
Show InChI InChI=1S/C18H16ClF2N3O2/c19-12-2-4-17(25)11(5-12)8-23-24-18(26)9-22-16-7-13(16)10-1-3-14(20)15(21)6-10/h1-6,8,13,16,22,25H,7,9H2,(H,24,26)/b23-8+/t13-,16+/m0/s1
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n/an/a 456n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231781
PNG
(CHEMBL4090528)
Show SMILES C(Sc1nc(Sc2ccccn2)c2nnn(Cc3ccccc3)c2n1)c1ccccc1
Show InChI InChI=1S/C23H18N6S2/c1-3-9-17(10-4-1)15-29-21-20(27-28-29)22(31-19-13-7-8-14-24-19)26-23(25-21)30-16-18-11-5-2-6-12-18/h1-14H,15-16H2
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n/an/a 564n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451579
PNG
(CHEMBL4210623)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1ccc(F)cc1 |r|
Show InChI InChI=1S/C19H18F3N3O/c1-11(12-2-5-14(20)6-3-12)24-25-19(26)10-23-18-9-15(18)13-4-7-16(21)17(22)8-13/h2-8,15,18,23H,9-10H2,1H3,(H,25,26)/b24-11+/t15-,18+/m0/s1
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n/an/a 631n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231773
PNG
(CHEMBL4069511)
Show SMILES C#CCSc1nc(Sc2ccccn2)c2nnn(Cc3ccccc3)c2n1
Show InChI InChI=1S/C19H14N6S2/c1-2-12-26-19-21-17-16(18(22-19)27-15-10-6-7-11-20-15)23-24-25(17)13-14-8-4-3-5-9-14/h1,3-11H,12-13H2
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n/an/a 678n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231771
PNG
(CHEMBL4087193)
Show SMILES CCCSc1nc(Sc2ccccn2)c2nnn(Cc3ccccc3)c2n1
Show InChI InChI=1S/C19H18N6S2/c1-2-12-26-19-21-17-16(18(22-19)27-15-10-6-7-11-20-15)23-24-25(17)13-14-8-4-3-5-9-14/h3-11H,2,12-13H2,1H3
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n/an/a 685n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231780
PNG
(CHEMBL4065771)
Show SMILES CCCSc1nc(Sc2ccccn2)c2nnn(CCc3cccs3)c2n1
Show InChI InChI=1S/C18H18N6S3/c1-2-11-26-18-20-16-15(17(21-18)27-14-7-3-4-9-19-14)22-23-24(16)10-8-13-6-5-12-25-13/h3-7,9,12H,2,8,10-11H2,1H3
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n/an/a 717n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231778
PNG
(CHEMBL4068480)
Show SMILES CCCSc1nc(Sc2ccccn2)c2nnn(Cc3ccco3)c2n1
Show InChI InChI=1S/C17H16N6OS2/c1-2-10-25-17-19-15-14(16(20-17)26-13-7-3-4-8-18-13)21-22-23(15)11-12-6-5-9-24-12/h3-9H,2,10-11H2,1H3
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n/an/a 758n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451584
PNG
(CHEMBL4209568)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1cc(Br)ccc1O |r|
Show InChI InChI=1S/C19H18BrF2N3O2/c1-10(13-7-12(20)3-5-18(13)26)24-25-19(27)9-23-17-8-14(17)11-2-4-15(21)16(22)6-11/h2-7,14,17,23,26H,8-9H2,1H3,(H,25,27)/b24-10+/t14-,17+/m0/s1
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n/an/a 828n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50451593
PNG
(CHEMBL4208534)
Show SMILES C\C(=N/NC(=O)CN[C@@H]1C[C@H]1c1ccc(F)c(F)c1)c1cc(Cl)ccc1O |r|
Show InChI InChI=1S/C19H18ClF2N3O2/c1-10(13-7-12(20)3-5-18(13)26)24-25-19(27)9-23-17-8-14(17)11-2-4-15(21)16(22)6-11/h2-7,14,17,23,26H,8-9H2,1H3,(H,25,27)/b24-10+/t14-,17+/m0/s1
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n/an/a 882n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of LSD1 (unknown origin)


Bioorg Med Chem Lett 27: 5036-5039 (2017)


Article DOI: 10.1016/j.bmcl.2017.10.003
BindingDB Entry DOI: 10.7270/Q2J105QD
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526215
PNG
(CHEMBL1192435)
Show SMILES Cc1cc(NN)n2nc(SCc3ccccc3)nc2n1
Show InChI InChI=1S/C13H14N6S/c1-9-7-11(17-14)19-12(15-9)16-13(18-19)20-8-10-5-3-2-4-6-10/h2-7,17H,8,14H2,1H3
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n/an/a 882n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231754
PNG
(CHEMBL4074390)
Show SMILES CCCSc1nc(Sc2ccccn2)c2nnn(CC(C)C)c2n1
Show InChI InChI=1S/C16H20N6S2/c1-4-9-23-16-18-14-13(20-21-22(14)10-11(2)3)15(19-16)24-12-7-5-6-8-17-12/h5-8,11H,4,9-10H2,1-3H3
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n/an/a 960n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231769
PNG
(CHEMBL4094875)
Show SMILES CCCSc1nc(Sc2ccccn2)c2nnn(C3CCCC3)c2n1
Show InChI InChI=1S/C17H20N6S2/c1-2-11-24-17-19-15-14(21-22-23(15)12-7-3-4-8-12)16(20-17)25-13-9-5-6-10-18-13/h5-6,9-10,12H,2-4,7-8,11H2,1H3
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n/an/a 1.15E+3n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524592
PNG
(CHEMBL4550944)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(F)cc2)c2ccc(Cl)cc12
Show InChI InChI=1S/C21H17ClFNO3/c1-12-18(11-27-21(12)26)20(25)17-10-24(9-13-2-5-15(23)6-3-13)19-7-4-14(22)8-16(17)19/h2-8,10,18,20,25H,1,9,11H2
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n/an/a 1.23E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526207
PNG
(CHEMBL4529482)
Show SMILES Cc1cc(NN)n2nc(SCc3csc4ccc(Cl)cc34)nc2n1
Show InChI InChI=1S/C15H13ClN6S2/c1-8-4-13(20-17)22-14(18-8)19-15(21-22)24-7-9-6-23-12-3-2-10(16)5-11(9)12/h2-6,20H,7,17H2,1H3
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n/an/a 1.61E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50523251
PNG
(CHEMBL4475385)
Show SMILES CN1CCN(CC1)c1ccc(Nc2cc(C)nc3nc(SCc4nc5ccccc5[nH]4)nn23)cc1
Show InChI InChI=1S/C25H27N9S/c1-17-15-23(27-18-7-9-19(10-8-18)33-13-11-32(2)12-14-33)34-24(26-17)30-25(31-34)35-16-22-28-20-5-3-4-6-21(20)29-22/h3-10,15,27H,11-14,16H2,1-2H3,(H,28,29)
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n/an/a 1.72E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 substrate by amplex red and horseradish peroxida...


Eur J Med Chem 167: 388-401 (2019)


Article DOI: 10.1016/j.ejmech.2019.02.039
BindingDB Entry DOI: 10.7270/Q2ST7T7R
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524624
PNG
(CHEMBL4470161)
Show SMILES Cc1ccc(cc1)S(=O)(=O)n1cc(C(O)C2COC(=O)C2=C)c2cc(Cl)ccc12
Show InChI InChI=1S/C21H18ClNO5S/c1-12-3-6-15(7-4-12)29(26,27)23-10-17(16-9-14(22)5-8-19(16)23)20(24)18-11-28-21(25)13(18)2/h3-10,18,20,24H,2,11H2,1H3
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n/an/a 1.78E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526193
PNG
(CHEMBL4455265)
Show SMILES Cc1cc(NN)n2nc(SCc3ccc(cc3)C(F)(F)F)nc2n1
Show InChI InChI=1S/C14H13F3N6S/c1-8-6-11(21-18)23-12(19-8)20-13(22-23)24-7-9-2-4-10(5-3-9)14(15,16)17/h2-6,21H,7,18H2,1H3
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n/an/a 2.32E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50231776
PNG
(CHEMBL4095820)
Show SMILES CCCSc1nc(Sc2ccccn2)c2nnn(CCO)c2n1
Show InChI InChI=1S/C14H16N6OS2/c1-2-9-22-14-16-12-11(18-19-20(12)7-8-21)13(17-14)23-10-5-3-4-6-15-10/h3-6,21H,2,7-9H2,1H3
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n/an/a 2.63E+3n/an/an/an/an/an/a



Key Laboratory of Technology of Drug Preparation (Zhengzhou University)

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21(DE) using H3K4me2 as substrate by fluorescence assay


ACS Med Chem Lett 8: 384-389 (2017)


Article DOI: 10.1021/acsmedchemlett.6b00423
BindingDB Entry DOI: 10.7270/Q2FQ9ZV3
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524625
PNG
(CHEMBL4545973)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(F)cc2)c2ccccc12
Show InChI InChI=1S/C21H18FNO3/c1-13-18(12-26-21(13)25)20(24)17-11-23(19-5-3-2-4-16(17)19)10-14-6-8-15(22)9-7-14/h2-9,11,18,20,24H,1,10,12H2
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n/an/a 4.47E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526204
PNG
(CHEMBL4527031)
Show SMILES Cc1cc(NN)n2nc(SCC#C)nc2n1
Show InChI InChI=1S/C9H10N6S/c1-3-4-16-9-12-8-11-6(2)5-7(13-10)15(8)14-9/h1,5,13H,4,10H2,2H3
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n/an/a 5.13E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524596
PNG
(CHEMBL4545461)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccccc2F)c2ccccc12
Show InChI InChI=1S/C21H18FNO3/c1-13-17(12-26-21(13)25)20(24)16-11-23(19-9-5-3-7-15(16)19)10-14-6-2-4-8-18(14)22/h2-9,11,17,20,24H,1,10,12H2
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n/an/a 5.85E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526196
PNG
(CHEMBL4572016)
Show SMILES Cc1cc(NN)n2nc(SCc3ccc(Cl)cc3)nc2n1
Show InChI InChI=1S/C13H13ClN6S/c1-8-6-11(18-15)20-12(16-8)17-13(19-20)21-7-9-2-4-10(14)5-3-9/h2-6,18H,7,15H2,1H3
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n/an/a 5.87E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524640
PNG
(CHEMBL4456313)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)nc2)c2ccccc12
Show InChI InChI=1S/C20H17ClN2O3/c1-12-16(11-26-20(12)25)19(24)15-10-23(17-5-3-2-4-14(15)17)9-13-6-7-18(21)22-8-13/h2-8,10,16,19,24H,1,9,11H2
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n/an/a 5.90E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526210
PNG
(CHEMBL4440289)
Show SMILES Cc1ccc(CSc2nc3nc(C)cc(NN)n3n2)cc1
Show InChI InChI=1S/C14H16N6S/c1-9-3-5-11(6-4-9)8-21-14-17-13-16-10(2)7-12(18-15)20(13)19-14/h3-7,18H,8,15H2,1-2H3
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n/an/a 6.16E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524598
PNG
(CHEMBL4591471)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)c(Cl)c2)c2ccccc12
Show InChI InChI=1S/C21H17Cl2NO3/c1-12-16(11-27-21(12)26)20(25)15-10-24(19-5-3-2-4-14(15)19)9-13-6-7-17(22)18(23)8-13/h2-8,10,16,20,25H,1,9,11H2
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n/an/a 6.58E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526197
PNG
(CHEMBL4443596)
Show SMILES Cc1cc(NN)n2nc(SCc3ccc(F)cc3)nc2n1
Show InChI InChI=1S/C13H13FN6S/c1-8-6-11(18-15)20-12(16-8)17-13(19-20)21-7-9-2-4-10(14)5-3-9/h2-6,18H,7,15H2,1H3
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n/an/a 8.13E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50526199
PNG
(CHEMBL4457116)
Show SMILES Cc1cc(NN)n2nc(SCC=C)nc2n1
Show InChI InChI=1S/C9H12N6S/c1-3-4-16-9-12-8-11-6(2)5-7(13-10)15(8)14-9/h3,5,13H,1,4,10H2,2H3
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n/an/a 8.21E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) using H3K4me2 as substrate by fluorescence assay


Eur J Med Chem 166: 432-444 (2019)


Article DOI: 10.1016/j.ejmech.2019.01.075
BindingDB Entry DOI: 10.7270/Q29S1VGB
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524602
PNG
(CHEMBL4592421)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)nc2)c2ccc(Cl)cc12
Show InChI InChI=1S/C20H16Cl2N2O3/c1-11-16(10-27-20(11)26)19(25)15-9-24(8-12-2-5-18(22)23-7-12)17-4-3-13(21)6-14(15)17/h2-7,9,16,19,25H,1,8,10H2
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n/an/a 8.34E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524603
PNG
(CHEMBL4439541)
Show SMILES COCCCOc1ccnc(Cn2cc(C(O)C3COC(=O)C3=C)c3cc(Cl)ccc23)c1C
Show InChI InChI=1S/C25H27ClN2O5/c1-15-20(14-33-25(15)30)24(29)19-12-28(22-6-5-17(26)11-18(19)22)13-21-16(2)23(7-8-27-21)32-10-4-9-31-3/h5-8,11-12,20,24,29H,1,4,9-10,13-14H2,2-3H3
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n/an/a 8.41E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
Lysine-specific histone demethylase 1A


(Homo sapiens (Human))
BDBM50524629
PNG
(CHEMBL4527359)
Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccccc2C(F)(F)F)c2ccccc12
Show InChI InChI=1S/C22H18F3NO3/c1-13-17(12-29-21(13)28)20(27)16-11-26(19-9-5-3-7-15(16)19)10-14-6-2-4-8-18(14)22(23,24)25/h2-9,11,17,20,27H,1,10,12H2
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n/an/a 8.96E+3n/an/an/an/an/an/a



Zhengzhou University

Curated by ChEMBL


Assay Description
Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...


Eur J Med Chem 175: 357-372 (2019)


Article DOI: 10.1016/j.ejmech.2019.04.065
BindingDB Entry DOI: 10.7270/Q2X351W0
More data for this
Ligand-Target Pair
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